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Time-dependent screening in a two-dimensional electron gas

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236 M. Alduc<strong>in</strong> et al. / Surface Science 559 (2004) 233–240<br />

q <strong>in</strong>d ðrÞ ¼ Z Z 1<br />

<br />

<br />

1<br />

1<br />

dqqJ 0 ðqrÞRe<br />

1 ;<br />

2p 0<br />

2D ðq; 0Þ<br />

ð5Þ<br />

which correspond to the stationary expression for<br />

the density <strong>in</strong>duced by an external charge density<br />

q ext ðrÞ ¼Z 1 dðrÞ. We checked that the results obta<strong>in</strong>ed<br />

by omitt<strong>in</strong>g the cos<strong>in</strong>e term <strong>in</strong> Eq. (4)<br />

reproduce well those obta<strong>in</strong>ed with Eq. (5). Notice,<br />

however, that <strong>in</strong> order to achieve this agreement it<br />

was necessary to use the exact x p ðqÞ <strong>in</strong>stead of the<br />

analytical approximations.<br />

3. Results and discussion<br />

Fig. 1. Spectrum of excitations for (a) 2D <strong>electron</strong> <strong>gas</strong> (upper<br />

panel) and (b) 3D <strong>electron</strong> <strong>gas</strong> (lower panel). In both cases<br />

r s ¼ 2. The shadow areas <strong>in</strong>dicate the ðq; xÞ-values at which the<br />

e-h pair excitations can take place. The curves x p ðqÞ <strong>in</strong>dicate<br />

the plasmon excitations.<br />

In the 2D case however, the plasmon frequency<br />

behaves as<br />

x 2 p ’ q2 F q<br />

for small values of q<br />

and as<br />

x 2 p ’ q2 F q þ 3=4q2 F q2 for larger values of q:<br />

There are <strong>two</strong> dist<strong>in</strong>ctive features for the 2Dplasmon<br />

frequency as compared to the 3D one: x p<br />

is zero for q ¼ 0 and the q-dispersion is stronger.<br />

Let us make a f<strong>in</strong>al comment on the expression<br />

we derived for the <strong>in</strong>duced density <strong>in</strong> Eq. (4). In<br />

the limit t !1, s<strong>in</strong>ce the cosðxtÞ term <strong>in</strong>tegrates<br />

to zero, the x-<strong>in</strong>tegral can be analytically evaluated<br />

us<strong>in</strong>g the Kramers–Kron<strong>in</strong>g relations. Hence,<br />

one gets<br />

In this section we show results for an external<br />

charge created <strong>in</strong> an <strong>electron</strong> <strong>gas</strong> with r s ¼ 2.<br />

Calculations were also carried out for different<br />

metallic densities (r s ¼ 3, 4). In general, we observe<br />

that for lower densities, the response of the medium<br />

to screen the external impurity is slower. Except<br />

for this fact, the comparative analysis between<br />

the 2D and the 3D <strong>electron</strong> <strong>gas</strong> presented <strong>in</strong> this<br />

section can be qualitatively generalized to those<br />

densities.<br />

In Fig. 2 we plot the <strong>electron</strong>ic density n <strong>in</strong>d ¼<br />

q <strong>in</strong>d <strong>in</strong>duced at the position of the suddenly created<br />

charge as a function of time t for a 2D (Fig.<br />

2(a), upper panel) and a 3D (Fig. 2(b), lower<br />

panel) <strong>electron</strong> <strong>gas</strong>. S<strong>in</strong>ce the spectral functions<br />

Imf1= RPA<br />

2D;3D<br />

g consist of a cont<strong>in</strong>uum part (e-h<br />

pair) and a plasmon mode, we calculate the <strong>in</strong>duced<br />

density as q <strong>in</strong>d ¼ q eh þ q pl , where q eh and q pl<br />

take <strong>in</strong>to account the contribution to the <strong>screen<strong>in</strong>g</strong><br />

process com<strong>in</strong>g from e-h and plasmon excitation,<br />

respectively. Accord<strong>in</strong>gly <strong>in</strong> Fig. 2, n <strong>in</strong>d (bold-solid<br />

l<strong>in</strong>e) is the sum of n eh (long-dashed l<strong>in</strong>e) and n pl<br />

(dotted l<strong>in</strong>e). The stationary value (t !1) is<br />

<strong>in</strong>dicated by a th<strong>in</strong>-solid l<strong>in</strong>e. As it may be seen<br />

from the figure, n <strong>in</strong>d ð0; tÞ is dom<strong>in</strong>ated by the e-h<br />

part that rises quite fast with<strong>in</strong> the first 2–3 a.u. of<br />

time. This behaviour is observed for both the 2D<br />

and the 3D medium. Nevertheless, an important<br />

difference arises between both cases. Whereas <strong>in</strong> a<br />

2D <strong>electron</strong> <strong>gas</strong> n <strong>in</strong>d reaches the stationary value at<br />

t 8–9 a.u., <strong>in</strong> the 3D case n <strong>in</strong>d oscillates around<br />

its stationary value even for the longest time

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